| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs587777893 | 0.658 | 0.240 | 1 | 11128107 | missense variant | G/A;T | snv | 67 | |||
| rs749203329 | 0.882 | 0.080 | 19 | 6213787 | missense variant | C/T | snv | 2.0E-05 | 1.4E-05 | 7 | |
| rs1567782714 | 0.882 | 0.120 | 16 | 57655528 | stop gained | C/T | snv | 5 | |||
| rs587783579 | 1.000 | 0.080 | X | 111401014 | frameshift variant | T/-;TT | delins | 2 | |||
| rs797045510 | X | 111410375 | frameshift variant | AA/- | delins | 1 | |||||
| rs797045512 | X | 111410119 | missense variant | T/C | snv | 1 | |||||
| rs797045513 | X | 111410083 | inframe insertion | -/GTA | delins | 1 | |||||
| rs797045514 | X | 111410059 | frameshift variant | -/G | delins | 1 | |||||
| rs797045515 | X | 111401167 | frameshift variant | A/- | delins | 1 | |||||
| rs797045518 | X | 111400995 | inframe insertion | -/TCCATCCAGAGTGTA | delins | 1 | |||||
| rs797045519 | X | 111410313 | frameshift variant | -/TAGGC | delins | 1 | |||||
| rs797045520 | X | 111330974 | frameshift variant | -/T | delins | 1 |